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Molecular reactivity of thiolate-protected noble metal nanoclusters: synthesis self-assembly and applications

机译:硫醇保护的贵金属纳米团簇的分子反应性:合成自组装和应用

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摘要

Thiolate-protected noble metal (e.g., Au and Ag) nanoclusters (NCs) are ultra-small particles with a core size of less than 3 nm. Due to the strong quantum confinement effects and diverse atomic packing modes in this ultra-small size regime, noble metal NCs exhibit numerous molecule-like optical, magnetic, and electronic properties, making them an emerging family of “metallic molecules”. Based on such molecule-like structures and properties, an individual noble metal NC behaves as a molecular entity in many chemical reactions, and exhibits structurally sensitive molecular reactivity to various ions, molecules, and other metal NCs. Although this molecular reactivity determines the application of NCs in various fields such as sensors, biomedicine, and catalysis, there is still a lack of systematic summary of the molecular interaction/reaction fundamentals of noble metal NCs at the molecular and atomic levels in the current literature. Here, we discuss the latest progress in understanding and exploiting the molecular interactions/reactions of noble metal NCs in their synthesis, self-assembly and application scenarios, based on the typical M(0)@M(i)–SR core–shell structure scheme, where M and SR are the metal atom and thiolate ligand, respectively. In particular, the continuous development of synthesis and characterization techniques has enabled noble metal NCs to be produced with molecular purity and atomically precise structural resolution. Such molecular purity and atomically precise structure, coupled with the great help of theoretical calculations, have revealed the active sites in various structural hierarchies of noble metal NCs (e.g., M(0) core, M–S interface, and SR ligand) for their molecular interactions/reactions. The anatomy of such molecular interactions/reactions of noble metal NCs in synthesis, self-assembly, and applications (e.g., sensors, biomedicine, and catalysis) constitutes another center of our discussion. The basis and practicality of the molecular interactions/reactions of noble metal NCs exemplified in this Review may increase the acceptance of metal NCs in various fields.
机译:硫醇化物保护的贵金属(例如,Au和Ag)纳米团簇(NCS)是超小颗粒,核心尺寸小于3nm。由于这种超小尺寸方案中的Quantum监禁效应和不同的原子包装模式,贵金属NCS表现出许多分子状光学,磁性和电子性质,使其成为新兴的“金属分子”系列。基于这种分子的结构和性质,个体贵金属NC在许多化学反应中表现为分子实体,并且对各种离子,分子和其他金属NCS表现出结构敏感的分子反应性。虽然该分子反应性决定了NCS在传感器,生物医学和催化等各种领域中的应用,但仍然缺乏贵金属NCS在当前文献中的分子和原子水平的分子相互作用/反应基础的系统概述。在这里,我们讨论了了解和利用贵金属NCS在其合成,自组装和应用方案中的最新进展,基于典型的M(0)@M(i)-SR核心壳结构其中M和Sr的方案分别是金属原子和硫醇酸酯配体。特别地,合成和表征技术的连续发展已经使具有以分子纯度和原子精确的结构分辨率产生的贵金属NC。这种分子纯度和原子精确的结构与理论计算的大量帮助相结合,揭示了贵金属NCS(例如,M(0)核,M-S界面和SR配体的各种结构等级中的活性位点分子相互作用/反应。在合成,自组装和应用(例如传感器,生物医学和催化中,贵金属NCS的这种分子相互作用/反应的解剖学构成了我们讨论的另一个中心。本综述中举例说明的贵金属NCS的分子相互作用/反应的基础和实用性可以增加各种领域的金属NC的接受。

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